ITGB7 integrin subunit beta 7

Information
Symbol
ITGB7
Type
protein-coding
Description
integrin subunit beta 7
Entrez Gene ID
3695
Genome
hg19
Position
chr12:53,585,107-53,601,035
Genome
hg38
Position
chr12:53,191,323-53,207,251
MIM
147559 OMIM
HGNC
HGNC:6162 HGNC
Ensembl
ENSG00000139626 Ensembl
Links
NCBI Gene Cards OncoKB
Clinical Significance
MGeND ClinVar
Benign 0 12
Likely benign 0 8
Uncertain significance 0 60
Ranking
ClinVar
0
0
0
80
0
Frequency
EXAC_EAS
EXAC_EAS
HGVD
HGVD
TOMMO
TOMMO
Gene
Position
EXAC_EAS
EXAC_EAS
HGVD
HGVD
TOMMO
TOMMO
Gene
Position
Disease area statistics
[No Data.]
Locus Zoom
Variants
Search Word
Target data :
MGeND data only
Category :
Search word :
Filtering :
Variant name Gene AA change CDS Japanese
frequency		 TogoVar MGeND Genome ClinVar CIViC evidence DisGeNET entry COSMIC
occurrence		 Prediction
Entry Origin Type Annotation Entry Origin Annotation
Search Word
Target data :
MGeND data only
Category :
Search word :
Filtering :
Name MGeND Type Genome Size Chromosome Start Stop Ref Alt ClinVar Origin Entry CIViC evidence DisGeNET entry
Entry Origin Type Annotation
Search Word
Target data :
MGeND data only
Category :
Search word :
Filtering :
Name MGeND Type Genome Gene symbol Chromosome Genomic start Genomic stop Strand Ref Alt ClinVar Origin Entry CIViC evidence DisGeNET entry
Entry Origin Type Annotation
TypeID
MIM 147559 OMIM
HGNC HGNC:6162 HGNC
Ensembl ENSG00000139626 Ensembl
AllianceGenome HGNC:6162
DescrptionSourceLinks
IDGenomeChromosomeStartEndLength
ENST00000267082.10 hg38 chr12 53,191,323 53,207,251 15,929
ENST00000550743.6 hg38 chr12 53,191,371 53,200,443 9,073
ENST00000422257.7 hg38 chr12 53,191,323 53,207,282 15,960
ENST00000267082.10 hg19 chr12 53,585,107 53,601,035 15,929
ENST00000422257.7 hg19 chr12 53,585,107 53,601,066 15,960
ENST00000550743.6 hg19 chr12 53,585,155 53,594,227 9,073
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